Canonical Allele Identifier: PA2825973572
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 432006
ClinVar RCV Id: RCV000497355 RCV002468583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157789.1:p.Gly361Asp
CA353335772
NM_001164317.2:c.1082G>A